dextromethorphan hbr-quinidine sulfate — Blue Cross Blue Shield of Illinois
pseudobulbar affect (PBA) associated with amyotrophic lateral sclerosis (ALS), multiple sclerosis (MS), dementia, stroke, or traumatic brain injury
Initial criteria
- The patient has a diagnosis of pseudobulbar affect (PBA)
- The patient has ONE of the following: amyotrophic lateral sclerosis (ALS) OR multiple sclerosis (MS) OR dementia OR stroke OR traumatic brain injury
- The prescriber has assessed the patient's PBA episodes (laughing and/or crying episodes) prior to therapy with the requested agent
- The prescriber is a specialist in the area of the patient’s diagnosis (e.g., neurologist, neuropsychologist, psychiatrist) OR has consulted with such a specialist
- The patient does NOT have any FDA labeled contraindications to the requested agent
Reauthorization criteria
- The patient has been previously approved for the requested agent through the plan’s Prior Authorization process
- The patient has had clinical benefit with the requested agent
- The prescriber is a specialist in the area of the patient’s diagnosis (e.g., neurologist, neuropsychologist, psychiatrist) OR has consulted with such a specialist
- The patient does NOT have any FDA labeled contraindications to the requested agent
Approval duration
12 months (BCBSIL); 3 months (others initial); 12 months (others renewal)